...
首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Lhx2/9 and Etv1 Transcription Factors have Complementary roles in Regulating the Expression of Guidance Genes slit1 and sema3a
【24h】

Lhx2/9 and Etv1 Transcription Factors have Complementary roles in Regulating the Expression of Guidance Genes slit1 and sema3a

机译:LHX2 / 9和ETV1转录因子具有互补的作用,用于调节指导基因的表达1和SEMA3A

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

During neural network development, growing axons read a map of guidance cues expressed in the surrounding tissue that lead the axons toward their targets. In particular, Xenopus retinal ganglion axons use the cues Slit1 and Semaphorin 3a (Sema3a) at a key guidance decision point in the mid-diencephalon in order to continue on to their midbrain target, the optic tectum. The mechanisms that control the expression of these cues, however, are poorly understood. Extrinsic Fibroblast Growth Factor (Fgf) signals are known to help coordinate the development of the brain by regulating gene expression. Here, we propose Lhx2/9 and Etv1 as potential downstream effectors of Fgf signalling to regulate slit1 and sema3a expression in the Xenopus forebrain. We find that lhx2/9 and etv1 mRNAs are expressed complementary to and within slit1/sema3a expression domains, respectively. Our data indicate that Lhx2 functions as an indirect repressor in that lhx2 overexpression within the forebrain downregulates the mRNA expression of both guidance genes, and in vitro lhx2/9 overexpression decreases the activity of slit1 and sema3a promoters. The Lhx2-VP16 constitutive activator fusion reduces sema3a promoter function, and the Lhx2-En constitutive repressor fusion increases slit1 induction. In contrast, etv1 gain of function transactivates both guidance genes in vitro and in the forebrain. Based on these data, together with our previous work, we hypothesize that Fgf signalling promotes both slit1 and sema3a expression in the forebrain through Etv1, while using Lhx2/9 to limit the extent of expression, thereby establishing the proper boundaries of guidance cue expression. (C) 2020 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:在神经网络开发期间,越来越多的轴突读了在周围组织中表达的引导线索的地图,以引领轴身朝向其目标。特别是,外爪疮视网膜神经节轴突在中间北alon的关键指导决策点处使用线索裂缝1和信号蛋白3a(sema3a),以便继续到它们的中脑目标,视神经结构。然而,控制这些提示表达的机制是较差的理解。已知外部成纤维细胞生长因子(FGF)信号通过调节基因表达来帮助协调脑的发育。在此,我们将LHX2 / 9和ETV1提出为FGF信号传导的潜在下游效应,以调节Xenopus前脑中的SlIT1和Sema3a表达。我们发现LHX2 / 9和ETV1 mRNA分别表达互补和在SLIT1 / SEMA3A表达域内。我们的数据表明,LHX2作为间接阻遏物的用途,即在前脑内的LHX2过表达下调两个引导基因的mRNA表达,并且体外LHX2 / 9过表达降低了SLIT1和SEMA3A启动子的活性。 LHX2-VP16组成型活化剂融合减少了SEMA3A启动子功能,LHX2-ZH组成型阻遏物融合增加了SLIT1诱导。相反,etv1功能在体外和前脑中转移两种引导基因。基于这些数据,与我们以前的工作一起,我们假设FGF信号传导通过ETV1促进前脑中的SLIT1和SEMA3A表达,同时使用LHX2 / 9来限制表达的程度,从而建立指导提示表达的适当界限。 (c)2020年度IBRO。 elsevier有限公司出版。保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号